1,2-Ethanedithiol → HCID 60167134, compound

HRID 1485830Notes

Reaction equation

HRID 1485830 reaction equation
C(S)CS.C([O:12][C:13]1[CH:14]=[C:15]([C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([F:35])[CH:30]=2)[C:16]([CH:19]2[CH2:24][CH:23]=[CH:22][CH2:21][CH:20]2[NH:25][C:26](=[O:28])[CH3:27])=[CH:17][CH:18]=1)C1C=CC=CC=1>C(Cl)Cl>[F:35][C:31]1[CH:30]=[C:29]([C:15]2[C:16]([CH:19]3[CH2:24][CH:23]=[CH:22][CH2:21][CH:20]3[NH:25][C:26](=[O:28])[CH3:27])=[CH:17][CH:18]=[C:13]([OH:12])[CH:14]=2)[CH:34]=[CH:33][CH:32]=1

Participants

4

Reactant 2

HCID 109021,2-EthanedithiolHCID 60167133HCID 60167133, compound

Product 1

HCID 60167134HCID 60167134, compoundYield 86%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

1,2-Ethanedithiol (0.22 mL, 2.66 mmol) and BF3OEt2 (0.176 mL, 1.4 mmol) were added to benzyl ether 18a (64 mg, 0.14 mmol) in DCM (1.8 mL). After 8 h, reaction mixture was concentrated and purified by column chromatography (SiO2, 10:100, MeOH:DCM) to afford phenol 19a as an amorphous solid (45 mg, 0.12 mmol, 86%)1H NMR (500 MHz, CDCl3) δ 8.98 (s, 1H), 7.40-7.34 (q, J=7.1, 6.2 Hz, 1H), 7.27 (d, J=7.6 Hz, 1H), 7.10-7.01 (m, 2H), 6.96 (d, J=9.4 Hz, 1H), 6.84-6.79 (dd, J=8.5, 2.6 Hz, 1H), 6.68 (d, J=2.6 Hz, 1H), 5.73-5.52 (m, 2H), 4.51-4.38 (dt, J=9.9, 5.0 Hz, 1H), 2.88-2.77 (q, J=9.5, 7.9 Hz, 1H), 2.43 (d, J=17.3 Hz, 1H), 2.34 (m, 2H), 2.18 (s, 1H), 1.77 (s, 3H); 13C NMR (125 MHz, CDCl3) δ 170.5, 163.6-161.7 (d, J=244.0 Hz), 155.2, 144.2 (d, J=7.6 Hz), 142.3, 130.8, 130.1 (d, J=8.4 Hz), 128.2, 127.0, 125.0 (d, J=2.2 Hz), 124.7, 116.5, 116.3 (d, J=20.3 Hz), 115.9, 114.2 (d, J=20.3 Hz, 49.6, 40.8, 35.5, 33.5, 23.2; HRMS (FAB) m/z: [M+Na+] for C21H25FNO2Na, 348.1376. found, 348.1379.

Workup

  1. customreaction mixture
  2. concentrationwas concentrated
  3. custompurified by column chromatography (SiO2, 10:100, MeOH:DCM)

Sources & evidence

ORD record
ord-bd6e49c1353c44478dca4fbd355cdc2d
Source dataset
uspto-grants-2016_08
Patent number
US09422320B2

Reaction notes

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